Advocacy Actions
Recommendation on Shandong Government Procurement Centre's Draft Document "Volume-based Centralised Procurement of High Value Medical Devices"
The Healthcare Equipment (HCE) Working Group submitted comments to the Shandong Government Procurement Centre's draft document "Volume-based Centralised Procurement of High Value Medical Devices".
Read moreMeeting with State Taxation Administration to discuss consumption tax on petrochemical products
On 18 December, representatives from the the Petrochemicals, Chemicals and Refining working group and the Finance and Taxation working group met with Mr Gong Jun from the State Taxation Administration to discuss consumption tax on petrochemical products.
Read moreMeeting with the Vice President of Shanghai High People's Court
On 16th December, Mr Carlo D’Andrea, Vice President and Chairman of the Shanghai Board together with the Dr Michael Tan, National Chair of the Legal Working Group as well as Mr Reinout van Malenstein, National Vice Chair of IPR Working Group met with Mr Mao Ronghua, Vice President of Shanghai High People's Court.
Read moreMeeting with the Centre of Medical Device Evaluation on Innovative Medical Device Registration
On 16 December, the Chamber attended the Innovative Medical Device Registration Meeting held by the Centre for Medical Device Evaluation.
Read moreMeeting with Environment center of Ministry of Ecology and Environment
Vice DG of the Center, MEE and EUCCC representatives did the introductions receptively and discussed about potential exchanges and cooperation.
Read moreWorkshop on Green and Circular Economy in China
The workshop provides an overview of the green and circular economy sector in China, its priorities for the 14th Five-year Plan period and the main challenges that European companies face in the industrial sectors.
Read moreSAMR Seminar on the Revision of Secondary Documents of Administrative Measures for Infant Formula Registration
On December 15th, representatives of Paediatric Nutrition Desk participant the meeting organized by the Special Food Administration and Supervision Department, State Administration for Market Regulation, on the revision of secondary documents of Administrative Measures for Infant Formula Registration.
Read moreComments on CMDE’s Public Consultation on the Technical Guidance on the Usage of Overseas Clinical Trial Data of In Vitro Diagnostic Reagents (Draft for Comments)
On 15 December, the medical device sector submitted the comments on the Technical Guidance on the Usage of Overseas Clinical Trial Data of In Vitro Diagnostic Reagents (Draft for Comments) published by the Centre for Medical Device Evaluation.
Read moreComments on the NMPA’s Public Consultation on the Dynamical Adjustment Working Procedure of Medical Device Classification Catalog (Draft for Comments)
On 15 December, the medical device sector sent comments on the Dynamical Adjustment Working Procedure of Medical Device Classification Catalog (Draft for Comments) released by the National Medical Products Administrtaion for public consultation.
Read moreMeeting with National Healthcare Security Administration on Cooperation in 2021
Meeting with National Healthcare Security Administration on Cooperation in 2021
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